Exploring Cleaning Verification/Validation Requirements While Introducing New Clinical or Commercial Products Into Multi-Product Pharmaceutical/Biopharmaceutical Manufacturing Facilities

Time: 3:30 pm
day: Conference Day One


  • Uncovering the challenges of new product introduction into multiproduct facilities
  • Evaluating the new product introduction's impact on the existing cleaning validation/verification program
  • Discussing different approaches to identify and reduce risk of cross-contamination due to new product introduction with limited toxicological information